CymitQuimica logo

CAS 89466-05-7

:

(3-amino-5-nitrophenyl)boronic acid

Description:
(3-Amino-5-nitrophenyl)boronic acid is an organic compound characterized by the presence of both an amino group and a nitro group attached to a phenyl ring, along with a boronic acid functional group. This compound typically appears as a solid at room temperature and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid moiety, which can form hydrogen bonds. The amino group provides basic properties, while the nitro group contributes to its electron-withdrawing characteristics, influencing its reactivity and potential applications in organic synthesis and medicinal chemistry. (3-Amino-5-nitrophenyl)boronic acid can participate in various chemical reactions, including Suzuki coupling, which is significant in the formation of carbon-carbon bonds. Its boronic acid functionality also allows it to interact with diols, making it useful in sensing applications and in the development of boron-based materials. Overall, this compound is of interest in both research and industrial applications due to its unique structural features and reactivity.
Formula:C6H7BN2O4
InChI:InChI=1/C6H7BN2O4/c8-5-1-4(7(10)11)2-6(3-5)9(12)13/h1-3,10-11H,8H2
SMILES:c1c(cc(cc1N)N(=O)=O)B(O)O
Synonyms:
  • boronic acid, B-(3-amino-5-nitrophenyl)-
  • (3-AMINO-5-NITROPHENYL)BORONIC ACID
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.